Davidson, A., Liskova, P., Evans, C., Dudakova, L., Nosková, L., Pontikos, N., . . . Hardcastle, A. (2016). Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2. Am J Hum Genet.
Citación estilo ChicagoDavidson, Alice E., et al. "Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused By Non-coding Mutations in the Promoter of OVOL2." Am J Hum Genet 2016.
Cita MLADavidson, Alice E., et al. "Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused By Non-coding Mutations in the Promoter of OVOL2." Am J Hum Genet 2016.
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